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A Polylactide Bioresorbable Scaffold Eluting Everolimus for Treatment of Coronary Stenosis: 5-Year Follow-Up.

机译:聚乳酸生物可吸收支架洗脱依维莫司治疗冠状动脉狭窄:5年随访。

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摘要

BACKGROUND\ud\udLong-term benefits of coronary stenosis treatment with an everolimus-eluting bioresorbable scaffold are unknown.\ud\udOBJECTIVES\ud\udThis study sought to evaluate clinical and imaging outcomes 5 years after bioresorbable scaffold implantation.\ud\udMETHODS\ud\udIn the ABSORB multicenter, single-arm trial, 45 (B1) and 56 patients (B2) underwent coronary angiography, intravascular ultrasound (IVUS), and optical coherence tomography (OCT) at different times. At 5 years, 53 patients without target lesion revascularization underwent final imaging.\ud\udRESULTS\ud\udBetween 6 months/1 year and 5 years, angiographic luminal late loss remained unchanged (B1: 0.14 ± 19 mm vs. 0.13 ± 0.33 mm; p = 0.7953; B2: 0.23 ± 0.28 mm vs. 0.18 ± 0.32 mm; p = 0.5685). When patients with a target lesion revascularization were included, luminal late loss was 0.15 ± 0.20 mm versus 0.15 ± 0.24 mm (p = 0.8275) for B1 and 0.30 ± 0.37 mm versus 0.32 ± 0.48 mm (p = 0.8204) for B2. At 5 years, in-scaffold and -segment binary restenosis was 7.8% (5 of 64) and 12.5% (8 of 64). On IVUS, the minimum lumen area of B1 decreased from 5.23 ± 0.97 mm(2) at 6 months to 4.89 ± 1.81 mm(2) at 5 years (p = 0.04), but remained unchanged in B2 (4.95 ± 0.91 mm(2) at 1 year to 4.84 ± 1.28 mm(2) at 5 years; p = 0.5). At 5 years, struts were no longer discernable by OCT and IVUS. On OCT, the minimum lumen area in B1 decreased from 4.51 ± 1.28 mm(2) at 6 months to 3.65 ± 1.39 mm(2) at 5 years (p = 0.01), but remained unchanged in B2, 4.35 ± 1.09 mm(2) at 1 year and 4.12 ± 1.38 mm(2) at 5 years (p = 0.24). Overall, the 5-year major adverse cardiac event rate was 11.0%, without any scaffold thrombosis.\ud\udCONCLUSIONS\ud\udAt 5 years, bioresorbable scaffold implantation in a simple stenotic lesion resulted in stable lumen dimensions and low restenosis and major adverse cardiac event rates. (ABSORB Clinical Investigation, Cohort B [ABSORB B]; NCT00856856).
机译:背景\ ud \ ud使用依维莫司洗脱生物可吸收支架治疗冠状动脉狭窄的长期益处尚不清楚。\ ud \ ud目标\ ud \ ud本研究旨在评估生物可吸收支架植入5年后的临床和影像学结果ud \ ud在ABSORB多中心单臂试验中,有45例(B1)和56例(B2)在不同时间接受了冠状动脉造影,血管内超声(IVUS)和光学相干断层扫描(OCT)。在第5年时,对53例无靶病变血运重建的患者进行了最终影像学检查。\ ud \ udRESULTS \ ud \ ud在6个月/ 1年和5年之间,血管造影的腔内晚期丢失保持不变(B1:0.14±19 mm vs. 0.13±0.33 mm ; p = 0.7953; B 2:0.23±0.28mm对0.18±0.32mm; p = 0.5685)。当包括具有目标病变血运重建的患者时,B1的腔内晚期丢失为0.15±0.20 mm,而B1为0.15±0.24 mm(p = 0.8275),B2为0.30±0.37 mm对0.32±0.48 mm(p = 0.8204)。在第5年时,支架内和节段二元再狭窄分别为7.8%(64个中的5个)和12.5%(64个中的8个)。在IVUS上,B1的最小管腔面积从6个月的5.23±0.97 mm(2)降低到5年时的4.89±1.81 mm(2)(p = 0.04),但在B2中保持不变(4.95±0.91 mm(2) )在1年时达到5.84±1.28 mm(2)在5年时; p = 0.5)。在5年时,OCT和IVUS不再能够识别支柱。在OCT上,B1的最小管腔面积从6个月的4.51±1.28 mm(2)降至5年的3.65±1.39 mm(2)(p = 0.01),但在B2则保持不变,为4.35±1.09 mm(2) )1年)和5年4.12±1.38 mm(2)(p = 0.24)。总体而言,5年主要不良心脏事件发生率为11.0%,没有任何支架血栓形成。结论在5年时,生物可吸收支架植入简单狭窄病变中可产生稳定的管腔尺寸,低再狭窄和重大不良反应。心脏事件发生率。 (ABSORB临床研究,队列B [ABSORB B]; NCT00856856)。

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